Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington.
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine and Program in Cellular and Molecular Biology, University of Michigan School of Medicine, Ann Arbor, Michigan.
Am J Respir Cell Mol Biol. 2022 Sep;67(3):284-308. doi: 10.1165/rcmb.2022-0089WS.
Clinical and molecular heterogeneity are common features of human disease. Understanding the basis for heterogeneity has led to major advances in therapy for many cancers and pulmonary diseases such as cystic fibrosis and asthma. Although heterogeneity of risk factors, disease severity, and outcomes in survivors are common features of the acute respiratory distress syndrome (ARDS), many challenges exist in understanding the clinical and molecular basis for disease heterogeneity and using heterogeneity to tailor therapy for individual patients. This report summarizes the proceedings of the 2021 Aspen Lung Conference, which was organized to review key issues related to understanding clinical and molecular heterogeneity in ARDS. The goals were to review new information about ARDS phenotypes, to explore multicellular and multisystem mechanisms responsible for heterogeneity, and to review how best to account for clinical and molecular heterogeneity in clinical trial design and assessment of outcomes. The report concludes with recommendations for future research to understand the clinical and basic mechanisms underlying heterogeneity in ARDS to advance the development of new treatments for this life-threatening critical illness.
临床和分子异质性是人类疾病的共同特征。了解异质性的基础,导致了许多癌症和肺部疾病如囊性纤维化和哮喘的治疗的重大进展。虽然在急性呼吸窘迫综合征(ARDS)的幸存者中,危险因素、疾病严重程度和结局的异质性是常见特征,但在理解疾病异质性的临床和分子基础以及利用异质性为个体患者定制治疗方面,仍然存在许多挑战。本报告总结了 2021 年阿斯彭肺会议的会议记录,该会议的目的是审查与理解 ARDS 临床和分子异质性相关的关键问题。目标是审查有关 ARDS 表型的新信息,探讨导致异质性的多细胞和多系统机制,并审查如何在临床试验设计和结局评估中最好地考虑临床和分子异质性。报告最后提出了未来研究的建议,以了解 ARDS 异质性的临床和基础机制,从而推进这种危及生命的严重疾病的新治疗方法的发展。